Reaktion #46167

ord-be4c3fb850964b1bb1e28c3c67e9cbba

Lösungsmittel

Reaktionsbedingungen

Temperatur
150°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    TemperaturThe mixture was cooled
  2. 2
    ExtraktionThe organic layer was extracted with ethyl acetate
  3. 3
    Trocknendried over anhydrous magnesium sulfate
  4. 4
    Einengenconcentrated
  5. 5
    Sonstigethe resulting residue was purified by column chromatography (ethyl acetate:hexane=1:3)

Vorschrift

2-Bromo-3-phenyl-6-(3-phenylpropoxy)indene-1-one (1.0 g, 2.3 mmol) was dissolved in N,N-dimethylformamide (10 ml). Copper (I) cyanide (617 mg, 6.9 mmol) was added thereto and the mixture was stirred for 3 hours at 150° C. The mixture was cooled, and saturated ammonium chloride was added thereto. The organic layer was extracted with ethyl acetate, dried over anhydrous magnesium sulfate, concentrated, and the resulting residue was purified by column chromatography (ethyl acetate:hexane=1:3) to obtain the title compound (700 mg, yield 80%) as a red solid.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07741323B2uspto-grants-2010_06